CRIS Current Research Information System

CERONI, FABIOLA
 Distribuzione geografica
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Continente #
NA - Nord America 694
EU - Europa 521
AS - Asia 301
AF - Africa 23
SA - Sud America 5
OC - Oceania 1
Totale 1.545
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Nazione #
US - Stati Uniti d'America 692
IT - Italia 236
CN - Cina 94
SG - Singapore 91
GB - Regno Unito 70
SE - Svezia 64
IN - India 45
DE - Germania 42
VN - Vietnam 28
IE - Irlanda 25
BG - Bulgaria 18
JO - Giordania 16
RU - Federazione Russa 11
TG - Togo 11
FR - Francia 10
FI - Finlandia 9
CH - Svizzera 7
CI - Costa d'Avorio 7
ID - Indonesia 7
PK - Pakistan 7
ES - Italia 6
UA - Ucraina 6
EE - Estonia 4
HK - Hong Kong 4
ZA - Sudafrica 4
AE - Emirati Arabi Uniti 3
BE - Belgio 3
BR - Brasile 3
CZ - Repubblica Ceca 3
NL - Olanda 3
CA - Canada 2
HR - Croazia 2
TR - Turchia 2
AT - Austria 1
AU - Australia 1
CL - Cile 1
CO - Colombia 1
IR - Iran 1
KR - Corea 1
LB - Libano 1
MD - Moldavia 1
PH - Filippine 1
SN - Senegal 1
Totale 1.545
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Città #
Singapore 88
Santa Clara 73
Chandler 72
Bologna 71
Southend 67
Fairfield 50
Ashburn 49
Redmond 32
Dublin 25
Houston 24
Princeton 24
Woodbridge 23
Boardman 22
Hyderabad 18
Sofia 18
Florence 17
New York 17
Amman 16
Wilmington 16
Seattle 15
Ann Arbor 14
Cambridge 13
Milan 13
Lomé 11
Helsinki 9
Abidjan 7
Berlin 7
Des Moines 7
Jakarta 7
Nanjing 7
Rome 7
San Diego 7
Beijing 6
Boydton 6
Guangzhou 6
Modena 6
Turin 6
Bern 5
Parma 5
Tappahannock 5
Cesena 4
Dong Ket 4
Dongguan 4
Hong Kong 4
Lahore 4
Padova 4
Shenyang 4
Westminster 4
Xi'an 4
Bari 3
Blacksburg 3
Brno 3
Brussels 3
Chengdu 3
Haikou 3
Munich 3
Salvador 3
Shanghai 3
Stockholm 3
Verona 3
Wuxi 3
Amsterdam 2
Aprilia 2
Aversa 2
Barcelona 2
Bremen 2
Dearborn 2
Dubai 2
Ferrara 2
Hangzhou 2
Harbin 2
Islamabad 2
Jinan 2
Konya 2
Lausanne 2
Medford 2
Modigliana 2
Monza 2
Nanchang 2
Nantong 2
Norwalk 2
Phoenix 2
Redwood City 2
Reggio Emilia 2
Rubano 2
Saint Petersburg 2
Salamanca 2
Sundbyberg 2
Vedelago 2
Washington 2
West Jordan 2
Ancona 1
Anguillara Sabazia 1
Arthurs Creek 1
Badalona 1
Baoding 1
Bogotá 1
Castel Maggiore 1
Cento 1
Changji 1
Totale 1.032
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Nome #
An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder. 244
A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder. 182
Contribution of CACNA1H Variants in Autism Spectrum Disorder Susceptibility 150
A deletion involving CD38 and BST1 results in a fusion transcript in a patient with autism and asthma. 110
Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment. 94
Biallelic variants in the small optic lobe calpain CAPN15 are associated with congenital eye anomalies, deafness and other neurodevelopmental deficits 73
Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidates 72
Contribution of compound heterozygous CACNA1H mutations in autism spectrum disorder susceptibility 72
New variant and expression studies provide further insight into the genotype-phenotype correlation in YAP1-related developmental eye disorders 70
Genome-wide analysis identifies a role for common copy number variants in specific language impairment 70
Multidisciplinary investigation links backward-speech trait and working memory through genetic mutation 69
null 63
New GJA8 variants and phenotypes highlight its critical role in a broad spectrum of eye anomalies 61
Genetics of anophthalmia and microphthalmia. Part 1: Non-syndromic anophthalmia/microphthalmia 60
De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies 54
Contribution of CACNA1H variants in Autism Spectrum Disorder Susceptibility 43
Analysis of Fibroblast Growth Factor 14 (FGF14) structural variants reveals the genetic basis of the early onset nystagmus locus NYS4 and variable ataxia 34
Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis' 34
Discovery of 42 genome-wide significant loci associated with dyslexia 27
Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people 20
Pathogenic variants in KMT2C result in a neurodevelopmental disorder distinct from Kleefstra and Kabuki syndromes 17
Totale 1.619
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Categoria #
all - tutte 4.789
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 4.789
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202090 0 0 0 0 0 16 15 19 27 6 3 4
2020/2021200 11 4 2 1 1 2 1 30 95 14 6 33
2021/2022310 20 4 27 9 39 11 4 20 15 21 94 46
2022/2023348 23 37 16 29 18 50 20 25 70 10 37 13
2023/2024185 14 28 10 19 18 44 4 3 12 7 13 13
2024/2025389 36 86 84 41 109 33 0 0 0 0 0 0
Totale 1.619